BG49273A3 - Method for preparing acryl acid - Google Patents
Method for preparing acryl acidInfo
- Publication number
- BG49273A3 BG49273A3 BG080624A BG8062487A BG49273A3 BG 49273 A3 BG49273 A3 BG 49273A3 BG 080624 A BG080624 A BG 080624A BG 8062487 A BG8062487 A BG 8062487A BG 49273 A3 BG49273 A3 BG 49273A3
- Authority
- BG
- Bulgaria
- Prior art keywords
- stage
- propylene
- acrolein
- mol
- diluent gas
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title 1
- -1 acryl Chemical group 0.000 title 1
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 8
- 239000007789 gas Substances 0.000 abstract 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 4
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- 239000002131 composite material Substances 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 239000011261 inert gas Substances 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000003134 recirculating effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Методът намира приложение в химическата промишленост. С него се подобряват селективността в окислителната реакция на пропилена до акролеин и окисляването на акролеина до акрилова киселина. Методът се състои в двуетапно каталитично окисление на пропилен, при който в първия етап се получава предимно акролеин, а във втория акрилова киселина чрез окисляване на акролеина, като се използват един или повече рециркулационни захранващи потоци, съдържащи кислород и инертен разреждащ газ или във всеки етап, или в двата. Разреждащият газ в първия етап съдържа от 0 до 0,4 мол вода пара/мол пропилен, а остатъкът от него представлява един или повече инертни газове. Разреждащият газ трябва да има съставен топлинен капацитет най-малко 6,5 кал/г-мол /с0/ при молно съотношение към пропилена от 2 до 32. Във втория етап газът съдържа един или повече инертни газове със съставен топлинен капацитет най-малко 6,5 кал/г-мол /с0/. 5 претенцииThe method finds application in the chemical industry. It improves the selectivity in the oxidation reaction of propylene to acrolein and the oxidation of acrolein to acrylic acid. The method consists of a two-stage catalytic oxidation of propylene, in which in the first stage acrolein is produced primarily and in the second stage acrylic acid is obtained by oxidizing acrolein using one or more recirculating feed streams containing oxygen and an inert diluent gas or in each stage , or in both. The diluent gas in the first stage contains from 0 to 0.4 moles of water vapor/mol of propylene, and the remainder is one or more inert gases. The diluent gas must have a composite heat capacity of at least 6.5 cal/g-mol /c0/ at a molar ratio to propylene of 2 to 32. In the second stage, the gas contains one or more inert gases with a composite heat capacity of at least 6 .5 cal/g-mol /c0/. 5 claims
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US88656286A | 1986-07-17 | 1986-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
BG49273A3 true BG49273A3 (en) | 1991-09-16 |
Family
ID=25389260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG080624A BG49273A3 (en) | 1986-07-17 | 1987-07-16 | Method for preparing acryl acid |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0253409B2 (en) |
JP (1) | JP2519942B2 (en) |
AT (1) | ATE69798T1 (en) |
BG (1) | BG49273A3 (en) |
CA (1) | CA1299193C (en) |
CS (1) | CS271344B2 (en) |
DE (1) | DE3774782D1 (en) |
ES (1) | ES2026495T5 (en) |
GR (2) | GR3003795T3 (en) |
MX (1) | MX169144B (en) |
Families Citing this family (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU606160B2 (en) * | 1987-05-27 | 1991-01-31 | Nippon Shokubai Kagaku Kogyo Co. Ltd. | Process for production of acrylic acid |
CA1327814C (en) * | 1988-09-26 | 1994-03-15 | William George Etzkorn | Anhydrous diluents for the isobutylene oxidation reaction to methacrolein and methacrolein oxidation to methacrylic acid |
US4999452A (en) * | 1989-05-15 | 1991-03-12 | Union Carbide Chemicals And Plastics Company Inc. | Process for producing acrylic ester |
JP2702864B2 (en) * | 1993-03-12 | 1998-01-26 | 株式会社日本触媒 | Catalyst regeneration method |
DE4431949A1 (en) * | 1994-09-08 | 1995-03-16 | Basf Ag | Process for the catalytic gas-phase oxidation of acrolein to acrylic acid |
DE4431957A1 (en) * | 1994-09-08 | 1995-03-16 | Basf Ag | Process for the catalytic gas-phase oxidation of propene to acrolein |
DE4436243A1 (en) | 1994-10-11 | 1996-04-18 | Basf Ag | Process for the separation of (meth) acrylic acid from the reaction gas mixture of the catalytic gas phase oxidation C¶3¶ / C¶4¶ compounds |
US5961790A (en) | 1994-12-14 | 1999-10-05 | Basf Aktiengesellschaft | Separation of (meth) acrylic acid by rectification |
DE19501325A1 (en) * | 1995-01-18 | 1996-07-25 | Basf Ag | Process for the rectificative separation of (meth) acrylic acid from a mixture containing (meth) acrylic acid |
DE19501326A1 (en) * | 1995-01-18 | 1996-07-25 | Basf Ag | Process for the rectificative separation of (meth) acrylic acid from a (meth) acrylic acid as the main constituent and lower aldehydes as minor constituents in a rectification column consisting of stripping section and rectifying section |
ES2135120T3 (en) * | 1995-03-10 | 1999-10-16 | Basf Ag | PROCEDURE FOR THE OXIDATION IN THE GASEOUS PHASE OF PROPYLENE TO ACROLEIN, ACRYLIC ACID, OR ITS MIXTURE, CONTINUOUSLY DONE, CATALYZED BY THE HETEROGENEOUS WAY. |
DE19600955A1 (en) | 1996-01-12 | 1997-07-17 | Basf Ag | Process for the preparation of acrylic acid and its esters |
DE19624674A1 (en) | 1996-06-20 | 1998-01-02 | Basf Ag | Process for the disposal of secondary components resulting from the production of acrylic acid or methacrylic acid |
DE19740252A1 (en) | 1997-09-12 | 1999-03-18 | Basf Ag | A novel method of acrylic and methacrylic acid production by catalytic gas oxidation of 3 - 4C hydrocarbons |
DE19810962A1 (en) * | 1998-03-13 | 1999-09-16 | Basf Ag | Reducing deposition in rectification to separate (meth)acrylic acid from higher boiling organic liquid |
DE19833049A1 (en) | 1998-07-22 | 2000-01-27 | Basf Ag | Acrylic acid production by gas-phase oxidation of 3C feedstock, involves work-up by condensation and vacuum-crystallization, recycling mother liquor and evaporated liquid to the condensation stage |
DE19902562A1 (en) | 1999-01-22 | 2000-07-27 | Basf Ag | Production of acrolein, useful as intermediate for glutardialdehyde, methionine, folic acid and acrylic acid, by catalytic oxidation of propene uses 2 consecutive reactors operating outside explosion range |
MY119958A (en) * | 1999-03-10 | 2005-08-30 | Basf Ag | Catalytic gas-phase oxidation of propene to acrylic acid |
MY121141A (en) | 1999-03-10 | 2005-12-30 | Basf Ag | Method for the catalytic gas-phase oxidation of propene into acrolein |
MY121878A (en) | 1999-03-10 | 2006-02-28 | Basf Ag | Method for the catalytic gas-phase oxidation of propene into acrylic acid |
DE19910508A1 (en) * | 1999-03-10 | 2000-09-21 | Basf Ag | Process of catalytic gas phase oxidation of acrolein to acrylic acid |
DE19926082A1 (en) | 1999-06-08 | 2000-12-14 | Basf Ag | Process for the purification and production of acrylic acid or methacrylic acid |
US6639106B1 (en) * | 1999-07-23 | 2003-10-28 | Rohm And Haas Company | Process for preparing and purifying acrylic acid from propylene having improved capacity |
DE19952964A1 (en) | 1999-11-03 | 2001-05-10 | Basf Ag | Process for the catalytic gas phase oxidation to (meth) acrolein and / or (meth) acrylic acid |
DE50108001D1 (en) | 2000-04-11 | 2005-12-15 | Basf Ag | PROCESS FOR CLEANING A CRUDE ACRYLIC MELT |
JP5021140B2 (en) | 2000-06-14 | 2012-09-05 | ビーエーエスエフ ソシエタス・ヨーロピア | Method for producing acrolein and / or acrylic acid |
DE10122027A1 (en) * | 2001-05-07 | 2002-05-23 | Basf Ag | Production of acrolein or acrylic acid involves absorption of propane and propene from a gas mixture followed by desorption and oxidation, with no catalytic dehydrogenation of propane and no added oxygen |
DE10031518A1 (en) | 2000-06-28 | 2002-01-10 | Basf Ag | Process for the preparation of hydroformylation products of propylene and of acrylic acid and / or acrolein |
DE10101695A1 (en) | 2001-01-15 | 2002-07-18 | Basf Ag | Heterogeneous catalyzed gas phase production of (meth)acrolein and/or meth(acrylic acid) using mixed oxide catalyst formed into geometrically shaped article of specific geometric characteristics |
DE10148566A1 (en) | 2001-10-01 | 2003-04-10 | Basf Ag | Process for the production of acrylic acid by heterogeneously catalyzed gas phase oxidation |
CN1260200C (en) | 2001-11-06 | 2006-06-21 | 三菱化学株式会社 | Method for collecting acrylic acid |
US7115776B2 (en) | 2002-07-18 | 2006-10-03 | Basf Aktiengesellschaft | Heterogeneously catalyzed gas-phase partial oxidation of at least one organic compound |
DE10237061A1 (en) | 2002-08-09 | 2004-02-19 | Basf Ag | Process for cleaning apparatus in which organic solvents containing (meth) acrylic acid have been treated and / or produced |
DE10313209A1 (en) | 2003-03-25 | 2004-03-04 | Basf Ag | Heterogeneously catalyzed partial gas phase oxidation of propene to acrylic acid, useful for the production of adhesive, comprises use of a gas phase mixture having a molar ratio of oxygen to propene of 1.5-2.5 |
FR2881136B1 (en) * | 2005-01-21 | 2007-03-23 | Arkema Sa | PROCESS FOR THE PREPARATION OF ACRYLIC ACID COMPRISING A PARTIAL OXIDATION OF PROPANE PROPYLENE |
DE102005019911A1 (en) | 2005-04-27 | 2006-11-02 | Basf Ag | Rectifying separation of a liquid II containing acrylic acid and/or methacrylic acid and acrolein and/or methacrolein and acetone, comprises providing the liquid II containing acetone to a rectification column |
DE102005062026A1 (en) * | 2005-12-22 | 2007-06-28 | Basf Ag | Catalytic partial gas phase oxidation of propylene to acrylic acid comprises introducing propylene, oxygen and inert dilution gas into first reaction zone, adding secondary gas and introducing the mixture into second reaction stage |
DE102005062010A1 (en) * | 2005-12-22 | 2007-06-28 | Basf Ag | Heterogeneously catalyzed partial gas phase oxidation of propylene to acrylic acid comprises introducing a reaction gas mixture into a reaction zone, and transferring the product gas mixture into a condensed phase and a separation zone |
DE102006000996A1 (en) | 2006-01-05 | 2007-07-12 | Basf Ag | Heterogeneously catalyzed gas phase partial oxidation of organic compound in fixed catalyst bed involves recovering quality of catalyst bed by replacing its portion, with a catalyst having activity lower than that of the replaced catalyst |
EP1734030A1 (en) | 2006-01-18 | 2006-12-20 | BASF Aktiengesellschaft | Method for long term operation of a heterogeneously catalysed gas phase partial oxidation of an organic educt |
FR2897059B1 (en) * | 2006-02-07 | 2008-04-18 | Arkema Sa | PROCESS FOR THE PREPARATION OF ACRYLIC ACID |
DE102008020688B3 (en) | 2008-04-24 | 2009-11-05 | Evonik Stockhausen Gmbh | Process for the preparation and purification of aqueous phases |
JP5433321B2 (en) * | 2009-06-30 | 2014-03-05 | 三菱レイヨン株式会社 | Method for producing (meth) acrylic acid |
DE102010042216A1 (en) | 2010-10-08 | 2011-06-09 | Basf Se | Inhibiting the unwanted radical polymerization of acrylic acid present in a liquid phase, comprises adding a chemical compound of copper to the liquid phase, and the liquid phase additionally contains propionic acid and glyoxal |
DE102011076931A1 (en) | 2011-06-03 | 2012-12-06 | Basf Se | Aqueous solution containing acrylic acid and its conjugate base |
US9150488B2 (en) * | 2012-06-22 | 2015-10-06 | Enerkem, Inc. | Production of acrylic acid and ethanol from carbonaceous materials |
US9738569B2 (en) | 2013-05-15 | 2017-08-22 | Enerkem, Inc. | Production of acrylic acid and ethanol from carbonaceous materials |
DE102014108273A1 (en) | 2014-06-12 | 2015-12-17 | Basf Se | Process and system for separating two-phase liquid mixtures |
US9815045B2 (en) | 2015-03-23 | 2017-11-14 | Clariant Corporation | Metal oxide catalyst material and processes for making and using same |
US9988324B2 (en) | 2015-11-04 | 2018-06-05 | Exxonmobil Chemical Patents Inc. | Process and system for making cyclopentadiene and/or dicyclopentadiene |
JP6776102B2 (en) * | 2016-11-21 | 2020-10-28 | 株式会社日本触媒 | Manufacturing method of water-absorbent resin using renewable raw materials |
US10479760B2 (en) | 2017-02-08 | 2019-11-19 | Clariant Corporation | Synthetic methods for the preparation of propylene ammoxidation catalysts |
US10479759B2 (en) | 2017-02-08 | 2019-11-19 | Clariant Corporation | Synthetic methods for the preparation of propylene ammoxidation catalysts |
US11447439B2 (en) | 2018-07-26 | 2022-09-20 | Basf Se | Method for inhibiting unwanted radical polymerisation of acrylic acid present in a liquid phase P |
EP3770145A1 (en) | 2019-07-24 | 2021-01-27 | Basf Se | A process for the continuous production of either acrolein or acrylic acid as the target product from propene |
US20230132285A1 (en) | 2020-03-26 | 2023-04-27 | Basf Se | Process for inhibiting the undesired free-radical polymerization of acrylic acid present in a liquid phase p |
WO2024089252A1 (en) | 2022-10-28 | 2024-05-02 | Basf Se | Process for the manufacture of a propylene-derived chemical of interest, in particular an acrylic ester, from renewably-sourced ethanol |
WO2024133081A1 (en) | 2022-12-20 | 2024-06-27 | Basf Se | Manufacture of an ethylene-derived chemical of interest, in particular acrylic acid, in combination with generation of heated steam |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2056614C3 (en) * | 1970-11-18 | 1981-04-16 | Basf Ag, 6700 Ludwigshafen | Process for the production of acrylic acid from propylene |
GB1467865A (en) * | 1973-07-27 | 1977-03-23 | Basf Ag | Catalytic oxidation or ammoxidation of a-olefins to alpha,beta- olefinically unsaturated aldehydes acids or nitriles |
DE2436818C3 (en) * | 1974-07-31 | 1985-05-09 | Basf Ag, 6700 Ludwigshafen | Process for the production of acrylic acid by oxidation of propylene with gases containing oxygen in two separate oxidation stages |
JPS5148609A (en) * | 1974-10-23 | 1976-04-26 | Asahi Glass Co Ltd | NIDANSANKANYORUISOPUCHIRENKARANO METAKU |
JPS52108917A (en) * | 1976-03-11 | 1977-09-12 | Nippon Shokubai Kagaku Kogyo Co Ltd | Preparation of acrylic acid by vapor-phase catalytic oxidation of prop ylene |
-
1987
- 1987-07-03 CA CA000541211A patent/CA1299193C/en not_active Expired - Lifetime
- 1987-07-16 BG BG080624A patent/BG49273A3/en unknown
- 1987-07-16 MX MX007388A patent/MX169144B/en unknown
- 1987-07-17 CS CS875443A patent/CS271344B2/en not_active IP Right Cessation
- 1987-07-17 DE DE8787110385T patent/DE3774782D1/en not_active Expired - Lifetime
- 1987-07-17 ES ES87110385T patent/ES2026495T5/en not_active Expired - Lifetime
- 1987-07-17 JP JP62177371A patent/JP2519942B2/en not_active Expired - Fee Related
- 1987-07-17 EP EP87110385A patent/EP0253409B2/en not_active Expired - Lifetime
- 1987-07-17 AT AT87110385T patent/ATE69798T1/en not_active IP Right Cessation
-
1992
- 1992-02-13 GR GR910401680T patent/GR3003795T3/el unknown
-
1999
- 1999-08-18 GR GR990402069T patent/GR3030991T3/en unknown
Also Published As
Publication number | Publication date |
---|---|
MX169144B (en) | 1993-06-23 |
GR3003795T3 (en) | 1993-03-16 |
JP2519942B2 (en) | 1996-07-31 |
ES2026495T5 (en) | 1999-08-16 |
EP0253409A2 (en) | 1988-01-20 |
EP0253409B1 (en) | 1991-11-27 |
GR3030991T3 (en) | 1999-12-31 |
EP0253409B2 (en) | 1999-06-09 |
EP0253409A3 (en) | 1988-10-05 |
CA1299193C (en) | 1992-04-21 |
CS544387A2 (en) | 1989-12-13 |
CS271344B2 (en) | 1990-09-12 |
DE3774782D1 (en) | 1992-01-09 |
ES2026495T3 (en) | 1992-05-01 |
ATE69798T1 (en) | 1991-12-15 |
JPS6393747A (en) | 1988-04-25 |
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